Result: solid dispersion method can effective promoting the dissolution.
结果：该法能很好的促进药物的释放。
OBJECTIVE The solid dispersion method was adopted to enhance the dissolution rate of nifedipine (NFDP) which is a poorly water-soluble drug.
目的采用制剂技术提高难溶性药物硝苯地平体外溶出速率。
Methods: HPMC and stearic acid were used to prepare melatonin controlled-release bilayer tablets by application of solid dispersion method and double compression technology.
方法：以hpmc、硬脂酸为骨架材料，采用固体分散技术和双层压片工艺，制备褪黑素双层控释片。
Method: Bomeolum Syntheticum and PEG 6000 mixing preparative solid dispersion and packed capsules, toxicity was tested.
方法：将冰片用水溶性辅料聚乙二醇6000制成固体分散体，并填装入胶囊，进行毒理试验。
The invention relates to a polyester amphipathic hyper-dispersant and a preparation method thereof to satisfy the demand of dispersion of solid particles in different polar media.
本发明涉及一种聚酯型两亲性超分散剂及其制备方法，以满足固体颗粒在不同极性介质中分散的需要。
Conclusion: Raman spectrometry which is fast, direct and non-destructive is an ideal method for examining the dispersivity of solid dispersion.
结论：拉曼光谱法快速、直接、对样品无损伤，是一种新的理想的检查固体分散体分散性的方法。
Conclusion: Raman spectrometry which is fast, direct and non-destructive is an ideal method in examining the dispersivity of solid dispersion.
结论：拉曼光谱法快速、直接、对样品无损伤，是一种新的理想的检查固体分散体分散性的方法。
The present invention relates to a tanshinone solid dispersion and its preparation method.
本发明提供了一种丹参酮固体分散物及其制备方法。
Methods: the solid dispersion was prepared by solvent method. The solubility, the dissolution rate and the derivative thermogravimetry (DTG) were determined.
方法：采用溶剂法制备固体分散体，进行溶解度、溶出速率测定，导数热重分析(DTG)。
The invention relates to a rolling mill and a method for treating viscous masses, in particular, for comminution and homogeneous dispersion of suspended solid particles in a binder.
本发明涉及用于处理粘性物质的、尤其是用于使粘合剂中的悬浮固体颗粒粉碎并均匀分布的的辊轧机和方法。
METHODS Preparing the solid dispersion by melting method at different drug-to-PEG ratios with different PEG moleculars and studying the preparation with dissolution rate in vitro and DSC method.
方法以不同分子量不同比例的聚乙二醇为载体，以熔融法制备固体分散体，并进行体外溶出度研究和DSC扫描。
Fenofibrate solid dispersion tablets were prepared by solvent melting method using PEG4000 and sodium lauryl sulfate.
PEG4000十烷硫酸钠体，溶剂-熔融制备非诺贝特固体散体，再适辅混合压片制非诺贝特固体散片。
Methods Etodolac solid dispersion was prepared with PEG as carrier by solvent-fusion method and identified by differential thermal analysis.
方法选用聚乙二醇为载体，采用溶剂-熔融法制备依托度酸固体分散体，通过差热分析对固体分散体进行鉴定。
Methods Etodolac solid dispersion was prepared with PEG as carrier by solvent-fusion method and identified by differential thermal analysis.
方法选用聚乙二醇为载体，采用溶剂-熔融法制备依托度酸固体分散体，通过差热分析对固体分散体进行鉴定。
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